Taiwan FDA registration e7bfa48ed6234e78ab1eef1608540424
"Shanghai Pigeon" Bofei bite record material
TW: “滬鴿”博飛咬合紀錄材
Taiwan·Risk Class 2·SHANDONG HUGE DENTAL MATERIAL CORPORATION·Registered Dec 22, 2022 – Dec 22, 2027ActiveRegistration details
- Analysis ID
- e7bfa48ed6234e78ab1eef1608540424
- Customs Code
- DHA09200142405
Company information
- Manufacturer
- SHANDONG HUGE DENTAL MATERIAL CORPORATION
- Manufacturer Country
- China
- Authorized Representative
- LEADING WAVE RA CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F.3660 Impression Material
- Import Information
- Chinese goods;; input
Dates and status
- Registration Date
- Dec 22, 2022
- Expiry Date
- Dec 22, 2027
About this record
Access comprehensive regulatory information for "Shanghai Pigeon" Bofei bite record material in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e7bfa48ed6234e78ab1eef1608540424 and manufactured by SHANDONG HUGE DENTAL MATERIAL CORPORATION. The authorized representative in Taiwan is LEADING WAVE RA CO., LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices